Structure Information
Structure

Compound Identification

SMILES

[H]C12CCCN1C(=O)C([H])(CC1=CC=CC=C1)N(C)C(=O)C([H])(CC1=CC=CC=C1)N=C(O)C([H])(C(C)C)N(C)C(=O)C([H])(OC(=O)C([H])(N(C)C(=O)C([H])(CC(C)C)N=C(O)C([H])(C(C)C)N(C)C(=O)C([H])(N=C2O)C(C)C)C(C)(C)O)C(C)C

InChIKey

InChIKey=IDERRMOEBWGLBD-UHFFFAOYSA-N

Formula

C58H88N8O11

Mass

1073.387

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Peptidomimetics

Subclass

Depsipeptides

Intermediate Tree Nodes

Not available

Direct Parent

Cyclic depsipeptides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Cyclic depsipeptide - Macrolide lactam - Alpha-amino acid ester - Macrolactam - Macrolide - Alpha-amino acid or derivatives - Monocyclic benzene moiety - Benzenoid - Pyrrolidine - Cyclic carboximidic acid - Tertiary alcohol - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Azacycle - Oxacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Organooxygen compound - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Alcohol - Carbonyl group - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

External Descriptors

Not available

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